Journal Information
Vol. 15. Issue 5.
Pages 436-441 (September - October 2011)
Share
Share
Download PDF
More article options
Vol. 15. Issue 5.
Pages 436-441 (September - October 2011)
Original article
Open Access
Molecular identification and typing of Mycobacterium massiliense isolated from postsurgical infections in Brazil
Visits
3188
Fernanda Monego1,
Corresponding author
fernandamonego@hotmail.com

Correspondence to: Universidade Federal do Paraná (UFPR) Depart. de Medicina Veterinária Rua dos Funcionários, 1540, Juveve 80035-050, Curitiba, Paraná,Brazil Phone.: +55 41 3350-5723 Fax: +55 41 3350-5623
, Rafael Silva Duarte2, Sueli Massumi Nakatani3, Wildo Navegantes Araújo4, Irina Nastassja Riediger5, Sonia Brockelt6, Verena Souza4, Jamyra Iglesias Cataldo7, Rubens Clayton da Silva Dias8, Alexander Welker Biondo9
1 PhD Student, Molecular and Cellular Biology, Universidade Federal do Paraná (UFPR), PR, Brazil
2 Associate Professor, Universidade Federal do Rio de Janeiro (UFRJ), RJ, Brazil
3 Head of Molecular Biology, Laboratório Central do Estado do Paraná (LACEN-PR), PR, Brazil
4 Epidemiologists, Secretaria de Vigilância em Saúde (SVS), Departament of Serological Vigilance, Brazil
5 Researcher, LACEN-PR, PR, Brazil
6 Head of the Mycobacteria Sector, LACEN-PR, PR, Brazil
7 PhD Student, Universidade do Estado do Rio de Janeiro (UERJ), RJ, Brazil
8 Researcher, UERJ, RJ, Brazil
9 Full Professor of Zoonoses, UFPR, PR, Brazil
Ver más
This item has received

Under a Creative Commons license
Article information
Abstract
Objective

One hundred thirty-one cases of postsurgical infections were reported in Southern Region of Brazil between August 2007 and January 2008. Thirty-nine (29.8%) cases were studied; this report describes epidemiological findings, species identification, antimicrobial susceptibility and clonal diversity of rapidly growing mycobacteria isolated in this outbreak.

Methods

All 39 isolates were analyzed by Ziehl-Nielsen stained smear, bacterial culture and submitted to rpoB partial gene sequencing for identification. The isolates were also evaluated for their susceptibility to amikacin, cefoxitin, clarithromycin, ciprofloxacin, doxycycline, tobramycin and sulfamethoxazole.

Results

Thirty-six isolates out of the confirmed cases were identified as Mycobacterium massiliense and the remaining three were identified as Mycobacterium abscessus, Mycobacterium chelonae and Mycobacterium fortuitum. All M. massiliense isolates were susceptible to amikacin (MIC90=8μg/mL) and clarithromycin (MIC90=0.25μg/mL) but resistant to cefoxitin, ciprofloxacin, doxycycline, tobramycin and sulfamethoxazole. Molecular analysis by pulsed-field gel electrophoresis clustered all 36 M. massiliense isolates and showed the same pattern (BRA 100) observed in three other outbreaks previously reported in Brazil.

Conclusions

These findings suggest a common source of infection for all patients and reinforce the hypotheses of spread of M. massiliense BRA100 in Brazilian hospital surgical environment in recent years.

Keywords:
mycobacteria, atypical
mycobacterium infections
microbiological analysis
Full text is only aviable in PDF
References
[1.]
J.K. Trupiano, B.A. Sebek, J. Goldfarb, et al.
Mastitis due to Mycobacterium abscessus after body piercing.
Clin Infect Dis, 33 (2001), pp. 131-134
[2.]
C. Viana-Niero, K.V. Lima, M.L. Lopes, et al.
Molecular characterization of Mycobacterium massiliense and Mycobacterium bolletii in isolates collected from outbreaks of infections after laparoscopic surgeries and cosmetic procedures.
J Clin Microbiol, 46 (2008), pp. 850-855
[3.]
B.A. Brown-Elliott, R.J. Wallace.
Clinical and taxonomic status of pathogenic nonpigmented or late-pigmenting rapidly growing mycobacteria.
Clin Microbiol Rev, 15 (2002), pp. 716-746
[4.]
Y. Zhibang, Z. BiXia, L. Qishan, et al.
Large-scale outbreak of infection with Mycobacterium chelonae subsp. abscessus after penicillin injection.
J Clin Microbiol, 40 (2002), pp. 2626-2628
[5.]
J. Esteban, N.Z. Martın-de-Hijas, A.I. Fernandez, et al.
Epidemiology of infections due to Non-pigmented Rapidly Growing Mycobacteria diagnosed in an urban area.
Eur J Clin Microbiol Infect Dis, 27 (2008), pp. 951-957
[6.]
H.Y. Kim, Y. Kook, Y.J. Yun, et al.
Proportions of Mycobacterium massiliense and Mycobacterium bolletii strains among Korean Mycobacterium chelonae-Mycobacterium abscessus group isolates.
J Clinl Microbiol, 46 (2008), pp. 3384-3390
[7.]
J.O. Falkinham.
Epidemiology of infection by nontuberculous mycobacteria.
Clin Microbiol Rev, 9 (1996), pp. 177-215
[8.]
T.S. Tiwari, B. Ray, K.C. Jost Jr., et al.
Forty years of disinfectant failure: outbreak of postinjection Mycobacterium abscessus infection caused by contamination of benzalkonium chloride.
Clin Infect Dis, 36 (2003), pp. 954-962
[9.]
R.W. Wilson, V.A. Steingrube, E.C. Bottger, et al.
Mycobacterium immunogenum sp. nov., a novel species related to Mycobacterium abscessus and associated with clinical disease, pseudooutbreaks and contaminated metalworking fluids: an international cooperative study on Mycobacterial taxonomy.
Int J Syst Evol Microbiol, 51 (2001), pp. 1751-1764
[10.]
V.J. Fraser, M. Jones, P.R. Murray, et al.
Contamination of flexible fibreoptic bronchoscopes with Mycobacterium chelonae linked to an automated bronchoscope disinfection machine.
Am Rev Resp Dis, 145 (1992), pp. 853-855
[11.]
D. Freitas, L. Alvarenga, J. Sampaio, et al.
An outbreak of Mycobacterium chelonae infection after LASIK.
Ophthalmol, 110 (2003), pp. 276-285
[12.]
J.L. Sampaio, E. Chimara, L. Ferrazoli, et al.
Application of four molecular typing methods for analysis of Mycobacterium fortuitum group strains causing post-mammaplasty infections.
Clin Microbiol Infect, 12 (2006), pp. 142-149
[13.]
R.S. Duarte, M.C. Lourenço, L. Fonseca, et al.
An Epidemic of Postsurgical Infections Caused by Mycobacterium massiliense.
J Clin Microbiol, 47 (2009), pp. 2149-2155
[14.]
A.M. Cardoso, E. Martins de Sousa, C. Viana-Niero, et al.
Emergence of nosocomial Mycobacterium massiliense infection in Goias.
Brazil. Microb Infect, 10 (2008), pp. 1552-1557
[15.]
D.N. McMurray.
Mycobacteria and nocardia.
Laboratory Procedures in Clinical Microbiology,
[16.]
R. Boom, C.J. Sol, M.M. Salimans, et al.
Rapid and simple method for purification of nucleic acids.
J Clin Microbiol, 28 (1990), pp. 495-503
[17.]
T. Adekambi, P. Colson, M. Drancourt.
rpoB-based identification of nonpigmented and late-pigmenting rapidly growing mycobacteria.
J Clin Microbiol, 41 (2003), pp. 5699-5708
[18.]
T.A. Hall.
BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT.
Nucleic Acids Symp, 41 (1999), pp. 95-98
[19.]
CLSI. Clinical and Laboratory Standards Institute Quality Manual, 3rd edn. CLSI, 940 West Valley Road, Suite 1400, Wayne, Pennsylvania 19087-1898 USA, 2003.
[20.]
N.V. Coleman, J.C. Spain.
Distribution of the coenzyme M pathway of epoxide metabolism among ethene- and vinyl chloride-degrading Mycobacterium strains.
Appl Environ Microbiol, 69 (2003), pp. 6041-6046
[21.]
J.L. Sampaio, C. Viana-Niero, D. de Freitas, et al.
Enterobacterial repetitive intergenic consensus PCR is a useful tool for typing Mycobacterium chelonae and Mycobacterium abscessus isolates.
Diagn Microbio Infect Dis, 55 (2006), pp. 107-118
[22.]
F.C. Tenover, R.D. Arbeit, R.V. Goering, et al.
Interpreting chromosomal DNArestriction patterns produced by pulsed-field gel electrophoresis: criteria for bacterial strain typing.
J Clin Microbiol, 33 (1995), pp. 2233-2239
[23.]
R.M. Donlan.
Biofilm formation: a clinically relevant microbiological process.
Clin Infect Dis, 33 (2001), pp. 1387-1392
[24.]
M. Simoes, M.O. Pereira, M.J. Vieira.
Effect of mechanical stress on biofilms challenged by different chemicals.
Water Res, 39 (2005), pp. 5142-5152
[25.]
N.Z. Martín-de-Hijas, D. García-Almeida, G. Ayala, et al.
Biofilm development by clinical strains of non-pigmented rapidly growing mycobacteria.
Clin Microbiol Infect, 15 (2009), pp. 931-936
[26.]
T.C. Mah, G.A. O’Toole.
Mechanisms of biofilm resistance to antimicrobial agents.
Trends Microbiol, 9 (2001), pp. 34-39
[27.]
M.A. De Groote, G. Huitt.
Infections due to rapidly growing mycobacteria.
Clin Infect Dis, 42 (2006), pp. 1756-1763
[28.]
J.R. Dalovisio, G.A. Pankey, R.J. Wallace.
Clinical usefulness of amikacin and doxycycline in the treatment of infection due to Mycobacterium fortuitum and Mycobacterium chelonae.
Rev Infect Dis, 3 (1981), pp. 1068-1074
Copyright © 2011. Elsevier Editora Ltda.. All rights reserved
Download PDF
The Brazilian Journal of Infectious Diseases
Article options
Tools